A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5496506



Internal ID273580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74050711..74051277hg38UCSC Ensembl
chr11:73761756..73762322hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17048360
Samples
Known GenesC2CD3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5496506
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer